NDC 76748-0475 Sanitize Nt-75

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76748-0475
Proprietary Name:
Sanitize Nt-75
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cri Tolling
Labeler Code:
76748
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76748-0475-1

Package Description: 204412 mL in 1 DRUM

NDC Code 76748-0475-2

Package Description: 1022000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

NDC Code 76748-0475-3

Package Description: 18921 mL in 1 PAIL

Product Details

What is NDC 76748-0475?

The NDC code 76748-0475 is assigned by the FDA to the product Sanitize Nt-75 which is product labeled by Cri Tolling. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 76748-0475-1 204412 ml in 1 drum , 76748-0475-2 1022000 ml in 1 container, flexible intermediate bulk , 76748-0475-3 18921 ml in 1 pail . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sanitize Nt-75?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Sanitize Nt-75 UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sanitize Nt-75 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".